Lithium iodide proves to be a very efficient catalyst for Michael addition of beta-dicarbonyl compounds. The successful application of this methodology to alpha,beta-unsaturated aldehydes allows an improved approach to 5,6-disubstituted cyclohex-2-en-1-ones.
LITHIUM IODIDE-CATALYZED CONJUGATE ADDITION OF BETA-DICARBONYL COMPOUNDS
ANTONIOLETTI R;
1991
Abstract
Lithium iodide proves to be a very efficient catalyst for Michael addition of beta-dicarbonyl compounds. The successful application of this methodology to alpha,beta-unsaturated aldehydes allows an improved approach to 5,6-disubstituted cyclohex-2-en-1-ones.File in questo prodotto:
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